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Interleukin-26 in Antibacterial Host Defense of Human Lungs Effects on Neutrophil Mobilization

Che, K. F. (författare)
Karolinska Institutet
Tengvall, Sara, 1977 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin,Institute of Medicine
Levanen, B. (författare)
Karolinska Institutet
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Silverpil, E. (författare)
Smith, Margaretha E. (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin,Institute of Medicine
Awad, M. (författare)
Vikstrom, M. (författare)
Palmberg, L. (författare)
Karolinska Institutet
Qvarfordt, Ingemar, 1954 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin,Institute of Medicine
Skold, M. (författare)
Karolinska Institutet
Lindén, Anders, 1961 (författare)
Karolinska Institutet,Gothenburg University,Göteborgs universitet,Institutionen för medicin,Institute of Medicine
visa färre...
 (creator_code:org_t)
2014
2014
Engelska.
Ingår i: American Journal of Respiratory and Critical Care Medicine. - 1073-449X .- 1535-4970. ; 190:9, s. 1022-1031
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Rationale: The role of the presumed Th17 cytokine IL-26 in antibacterial host defense of the lungs is not known. Objectives: To characterize the role of IL-26 in antibacterial host defense of human lungs. Methods: Intrabronchial exposure of healthy volunteers to endotoxin and vehicle was performed during bronchoscopy and bronchoalveolar lavage (BAL) samples were harvested. Intracellular IL-26 was detected using immunocytochemistry and immunocytofluorescence. This IL-26 was also detected using flow cytometry, as was its receptor complex. Cytoldnes and phosphorylated signal transducer and activator of transcription (STAT) 1 plus STAT3 were quantified using ELISA. Gene expression was analyzed by real-time polymerase chain reaction and neutrophil migration was assessed in vitro. Measurements and Main Results: Extracellular IL-26 was detected in BAL samples without prior exposure in vivo and was markedly increased after endotoxin exposure. Alveolar macrophages displayed gene expression for, contained, and released IL-26. Th and cytotoxic T cells also contained IL-26. In the BAL samples, IL-26 concentrations and innate effector cells displayed a correlation. Recombinant IL-26 potentiated neutrophil chemotaxis induced by IL-8 and fMLP but decreased chemokinesis for neutrophils. Myeloperoxidase in conditioned media from neutrophils was decreased. The IL-26 receptor complex was detected in neutrophils and IL-26 decreased phosphorylated STAT3 in these cells. In BAL and bronchial epithelial cells, IL-26 increased gene expression of the IL-26 receptor complex and STAT1 plus STAT3. Finally, IL-26 increased the release of neutrophil-mobilizing cytokines in BAL but not in epithelial cells. Conclusions: This study implies that alveolar macrophages produce IL-26, which stimulates receptors on neutrophils and focuses their mobilization toward bacteria and accumulated immune cells in human lungs.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)

Nyckelord

IL-10
infection
inflammation
macrophage
T cell
COMMUNITY-ACQUIRED PNEUMONIA
T-CELLS
AIRWAY INFLAMMATION
CONVERTING-ENZYME
EPITHELIAL-CELLS
FAMILY-MEMBERS
IL-10 FAMILY
TNF-ALPHA
GM-CSF
RECRUITMENT
Critical Care Medicine
Respiratory System

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